Alpha 1-antitrypsin deficiency in patients with chronic obstructive pulmonary disease patients: is systematic screening necessary?

OBJECTIVE: Alpha-1-antitrypsin deficiency is a relatively prevalent, but under-diagnosed, genetic disease. The objective of this study was to assess whether the systematic screening for alpha-1-antitrypsin deficiency in all patients with chronic obstructive pulmonary disease from a tertiary service...

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Detalles Bibliográficos
Autores principales: da Costa, Cláudia Henrique, Noronha Filho, Arnaldo José, Marques e Silva, Rosa Maria Fernambel, da Cruz, Thaís Ferrari, de Oliveira Monteiro, Valeria, Pio, Margareth, Rufino, Rogério Lopes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329068/
https://www.ncbi.nlm.nih.gov/pubmed/30630519
http://dx.doi.org/10.1186/s13104-018-4043-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329068/
https://www.ncbi.nlm.nih.gov/pubmed/30630519
http://dx.doi.org/10.1186/s13104-018-4043-9

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